QC Sample Management Technician — Data & Inventory

Bristol-Myers Squibb; Harvard (MA); On-site; USD 50,000 - 61,000; Full time

Job summary

Bristol Myers Squibb in Devens, MA is seeking a QC Sample Management Technician to oversee the movement and control of in-process, final product and stability samples within the QC laboratories. The role involves sample collection, inventory control, chain of custody, and timely sample delivery.

The position requires knowledge of GMP, can work 12-hour shifts, and involves data handling, documentation review, and collaboration with cross-functional teams.

Qualifications

• Ability to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements.
• Knowledge of LIMS, ELN and laboratory data analysis systems preferred.
• Problem-solving ability/mentality, technically adept and logical.
• Ability to communicate effectively with peers, department management and cross-functional peers.
• Experience with writing technical documents preferred.
• Ability to work in a fast-paced team environment, meet deadlines, and prioritize work.

Responsibilities

• Perform routine management of in-process, final product and stability samples and QC data throughout the sample lifecycle from receipt to disposition.
• Performs periodic sample and data inventory maintenance activities.
• Performs data compilation and review of GMP documentation in support of method trending.
• Compiles lot files for QC disposition review.
• Generate SOTR and manual CoA.
• Support document revision, project, CAPA and deviation/ investigation related tasks and/ or continuous improvement efforts.
• Train analysts on general job duties.
• Perform other tasks/duties as assigned.

Skills

Regulatory cGMP

LIMS/ELN

Documentation

Communication

Technical writing

Team work

Education

Bachelor's degree or equivalent

Science background preferred

Job description

Bristol Myers Squibb in Devens, MA is seeking a QC Sample Management Technician to oversee the movement and control of in-process, final product and stability samples within the QC laboratories. The role involves sample collection, inventory control, chain of custody, and timely sample delivery.

The position requires knowledge of GMP, can work 12-hour shifts, and involves data handling, documentation review, and collaboration with cross-functional teams.